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Endohead

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
Endohead FDA UDI
Generic Name
Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Device Name
Medacta Endo Head Ø 42, S FDA UDI
Model / Reference
01.25.242S FDA UDI
Description
Medacta Endo Head Ø 42, S FDA UDI

Identifiers

Primary DI / UDI-DI
07630030806285 FDA UDI
510(k) Number
K111145 FDA UDI
FDA Product Code
LZY FDA UDI
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bipolar femoral head outer component, hemiarthroplasty

Endohead by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bipolar femoral head outer component, hemiarthroplasty.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55b28f5c-2178-4b0c-be38-75562a458606 34 fields · synced May 30, 2026